4.3 Review

Metastatic Renal Cell Carcinoma Management

Journal

INTERNATIONAL BRAZ J UROL
Volume 35, Issue 3, Pages 256-270

Publisher

BRAZILIAN SOC UROL
DOI: 10.1590/S1677-55382009000300002

Keywords

renal cell carcinoma; neoplasm metastasis; anti angiogenetic agents; therapy

Funding

  1. Roche
  2. Bayer
  3. Wyeth
  4. Pfizer
  5. Inate
  6. Antigenics

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Purpose: To assess the current treatment of metastatic renal cell carcinoma, focusing on medical treatment options. Material and Methods: The most important recent publications have been selected after a literature search employing PubMed using the search terms: advanced and metastatic renal cell carcinoma, anti-angiogenesis drugs and systemic therapy; also significant meeting abstracts were consulted. Results: Progress in understanding the molecular basis of renal cell carcinoma, especially related to genetics and angiogenesis, has been achieved mainly through of the study of von Hippel-Lindau disease. A great variety of active agents have been developed and tested in metastatic renal cell carcinoma (mRCC) patients. New specific molecular therapies in metastatic disease are discussed. Sunitinib, Sorafenib and Bevacizumab increase the progression-free survival when compared to therapy with cytokines. Temsirolimus increases overall survival in high-risk patients. Growth factors and regulatory enzymes, such as carbonic anhydrase IX may be targets for future therapies. Conclusions: A broader knowledge of clear cell carcinoma molecular biology has permitted the beginning of a new era in mRCC therapy. Benefits of these novel agents in terms of progression-free and overall survival have been observed in patients with mRCC, and, in many cases, have become the standard of care. Sunitinib is now considered the new reference first-line treatment for mRCC. Despite all the progress in recent years, complete responses are still very rare. Currently, many important issues regarding the use of these agents in the management of metastatic renal cancer still need to be properly addressed.

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